- Utilises case studies to highlight the processes involved in receiving regulatory approval for new agricultural products
- Highlights the need for consistent regulation of genome-edited crops/products from country to country
- Reviews recent advances in plant protection regulations in the EU, focussing on those applicable to biopesticides and bioprotectants
Tabla de materias
- Chapter 1 – Creating a regulatory framework for cultured meat products: Singapore: Johnny Yeung, Yong Quan Tan, Siew Herng Chan, Kern Rei Chng, Calvin Yeo, Jer Lin Poh, Teng Yong Low and Joanne Sheot Harn Chan, National Centre for Food Science, Singapore;
- 1 Introduction
- 2 Key food safety issues in Singapore
- 3 The Singapore Food Agencys regulatory framework for cultured meat
- 4 Strengthening food safety capabilities in cultured meat products through partnerships
- 5 Building consumer confidence in the safety of cultured meat products
- 6 Conclusion
- 7 References
Chapter taken from: Post, M., Connon, C. and Bryant, C. (ed.), Advances in cultured meat technology, Burleigh Dodds Science Publishing, Cambridge, UK, 2023, (ISBN: 978 1 80146 376 8)
- Chapter 2 – The regulation of genome-edited crops: Gregory Jaffe, Center for Science in the Public Interest, USA;
- 1 Introduction
- 2 Background on genome editing and its regulation
- 3 Whether the Cartagena Biosafety Protocol applies to genome-edited crops
- 4 Country case studies demonstrating regulation of genome-edited crops
- 5 Analysis of regulations in different countries
- 6 Conclusion and future trends
- 7 References
Chapter taken from: Willmann, M. R. (ed.), Genome editing for precision crop breeding, Burleigh Dodds Science Publishing, Cambridge, UK, 2021, (ISBN: 978 1 78676 447 8)
- Chapter 3 – Key issues in the regulation of microbial bioprotectants in the European Union: challenges and solutions to achieve more sustainable crop protection: Rüdiger Hauschild, APIS Applied Insect Science Gmb H, Germany; and Willem J. Ravensberg, Koppert Biological Systems, The Netherlands;
- 1 Introduction
- 2 Issues of the administrative registration procedure in the European Union
- 3 Issues and solutions for the data requirements for microbial bioprotectants
- 4 New research, novel products and application methods
- 5 Conclusion and future trends
- 6 References
Chapter taken from: Köhl, J. and Ravensberg, W. (ed.), Microbial bioprotectants for plant disease management, Burleigh Dodds Science Publishing, Cambridge, UK, 2022, (ISBN: 978 1 78676 813 1)
- Chapter 4 – Improving regulatory approval processes for biopesticides and other new biological technologies in agriculture: Wyn Grant, University of Warwick, UK; and Roma Gwynn, Biorationale, UK;
- 1 Introduction
- 2 Establishing a regulatory framework for biopesticides
- 3 Pesticide regulation in the European Union (EU)
- 4 The development of the biopesticide sector and new regulatory requirements
- 5 Challenges in improving the regulatory framework for biopesticides
- 6 Current EU regulation of biopesticides
- 7 Global national initiatives in biopesticide regulation
- 8 Developing good regulatory practice
- 9 Conclusions
- 10 Where to look for further information
- 11 References
Chapter taken from: Birch, N. and Glare, T. (ed.), Biopesticides for sustainable agriculture, Burleigh Dodds Science Publishing, Cambridge, UK, 2019, (ISBN: 978 1 78676 356 3)
- Chapter 5 – Developing effective product dossiers for regulatory approval of new animal feed products: Manfred Lützow, saqual Gmb H, Switzerland;
- 1 Introduction: what are feed products?
- 2 The food chain: the product life cycle for feed ingredients
- 3 Safe feed and safe food
- 4 Where do you start?
- 5 Building the dossier
- 6 Characterisation and properties
- 7 Safety data: animals, consumers, workers and the environment
- 8 Effects and efficacy
- 9 Substantiating claims
- 10 Dossier submission and follow-up
- 11 Continuously updating the file
- 12 Where to look for further information
- 13 References
Chapter taken from: Navaratnam, P. (ed.), Developing animal feed products, Burleigh Dodds Science Publishing, Cambridge, UK, 2021, (ISBN: 978 1 78676 463 8)
Sobre el autor
Dr Willem J. Ravensberg is Corporate Senior Regulatory and Governmental Affairs Manager at Koppert Biological Systems. A leading expert in biocontrol product development, he is former President of the International Biocontrol Manufacturers Association (IBMA) and Bio Protection Global (BPG) which brings together the world’s leading biocontrol associations.